A study in subjects with rare inherited eye conditions caused by gene mutations to see if treatment with QLT091001 is safe and works to improve subjects' vision. A study in subjects with rare inherited eye conditions caused by gene mutations to see if treatment ...
A Study of the Efficacy and Safety of QLT091001 in Subjects with Inherited Retinal Disease (IRD) Caused by Mutation in Retinal Pigment Epithelium Protein 65 (RPE65) or Lecithin:Retinol Acyltransferase (LRAT) A Study of the Efficacy and Safety of QLT091001 in Subjects with Inherited Retinal Disease (IRD) Cau ...
Inherited retinal disease (IRD) phenotypically diagnosed as Leber congenital amaurosis (LCA) or retinitis pigmentosa (RP) caused by mutations in the retinal pigment epithelium protein 65 (RPE65) or lecithin:retinol acyltransferase (LRAT) genes MedDRA version: 19.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders MedDRA version: 19.0;Classification code 10070667;Term: Leber's congenital amaurosis;System Organ Class: 10010331 - Congenital, familial and genetic disorders ;Therapeutic area: Diseases [C] - Eye Diseases [C11] Inherited retinal disease (IRD) phenotypically diagnosed as Leber congenital amaurosis (LCA) or reti ...
Product Name: QLT091001 Product Code: QLT091001 INN or Proposed INN: ZuretinolAcetate Other descriptive name: QLT091001 Product Name: QLT091001 Product Code: QLT091001 INN or Proposed INN: ZuretinolAcetate Other descriptiv ...
A study in subjects with rare inherited eye conditions caused by gene mutations to see if treatment with QLT091001 is safe and works to improve subjects' vision. A study in subjects with rare inherited eye conditions caused by gene mutations to see if treatment ...
A Study of the Efficacy and Safety of QLT091001 in Subjects with Inherited Retinal Disease (IRD) Caused by Mutation in Retinal Pigment Epithelium Protein 65 (RPE65) or Lecithin:Retinol Acyltransferase (LRAT) A Study of the Efficacy and Safety of QLT091001 in Subjects with Inherited Retinal Disease (IRD) Cau ...
Inherited retinal disease (IRD) phenotypically diagnosed as Leber congenital amaurosis (LCA) or retinitis pigmentosa (RP) caused by mutations in the retinal pigment epithelium protein 65 (RPE65) or lecithin:retinol acyltransferase (LRAT) genes MedDRA version: 19.0;Level: PT;Classification code 10038914;Term: Retinitis pigmentosa;System Organ Class: 10010331 - Congenital, familial and genetic disorders MedDRA version: 19.0;Classification code 10070667;Term: Leber's congenital amaurosis;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Eye Diseases [C11] Inherited retinal disease (IRD) phenotypically diagnosed as Leber congenital amaurosis (LCA) or reti ...
Product Name: QLT091001 Product Code: QLT091001 INN or Proposed INN: ZuretinolAcetate Other descriptive name: QLT091001 Product Name: QLT091001 Product Code: QLT091001 INN or Proposed INN: ZuretinolAcetate Other descriptiv ...
QLT Inc.
NULL
Not Recruiting
Female: yes Male: yes
48
Phase 3
United States;France;Canada;Brazil;Denmark;Netherlands;Germany;United Kingdom;Switzerland